Overview
Assistant QA/QC Manager Jobs in Rayong, Thailand at Aditya Birla Chemicals
Title: Assistant QA/QC Manager
Company: Aditya Birla Chemicals
Location: Rayong, Thailand
Company Description Aditya Birla Chemicals, a part of the Aditya Birla Group, delivers application-focused chemical solutions with a strong emphasis on innovation and sustainability. With 19 manufacturing units, including 15 chemical plants, the company serves over 1,000 customers in 100 countries and operates 8 Application Development Centres across 4 countries. Its portfolio of more than 25 trusted brands reinforces leadership in Chlor-Alkali, Advanced Materials, Phosphate, and Sulphite businesses, along with Fashion Yarn (VFY) and Insulators. A passionate workforce of over 14,000 employees supports a diverse, high-performance environment focused on circularity and customer-first solutions. Joining Aditya Birla Chemicals means contributing to a global vision of sustainable, impactful, and innovative solutions.
Role Description The Assistant QA/QC Manager is a full-time, on-site role based in Rayong, Thailand. This role supports the quality leadership team in ensuring that all products, processes, and materials comply with internal standards, customer requirements, and regulatory guidelines. Day-to-day responsibilities include monitoring production quality, supervising routine inspections and laboratory testing, reviewing and updating quality procedures, and assisting in the investigation and resolution of non-conformances. The role also involves coordinating with production, maintenance, and supply chain teams to implement corrective and preventive actions, supporting audits, and preparing quality documentation and reports. The Assistant QA/QC Manager will help drive continuous improvement initiatives, promote safety and compliance, and provide guidance to QA/QC staff to maintain consistent quality performance.
Qualifications
- Strong foundation in quality assurance and quality control methodologies, including inspection, testing, documentation, and root cause analysis.
- Knowledge of chemical manufacturing processes, product specifications, and safety standards relevant to industrial chemical operations.
- Experience with quality management systems and regulatory compliance (e.g., ISO standards, environmental and occupational health regulations).
- Proficiency in data analysis, report preparation, and use of basic QA/QC tools and software for monitoring quality metrics.
- Effective communication, collaboration, and stakeholder management skills to work with cross-functional teams and external auditors.
- Demonstrated ability to lead or supervise teams, prioritize tasks, and manage multiple quality initiatives in a fast-paced environment.
- Bachelor’s degree or higher in Chemistry or a related technical discipline; advanced training in quality management is an advantage.
- Relevant experience in QA/QC within chemical, process, or manufacturing industries; prior experience in a multinational or large-scale operation is beneficial.
- Commitment to safety, sustainability, and continuous improvement, with a proactive approach to problem-solving and process optimization.
- Essential: In-depth, practical knowledge and working experience with ISO/IEC 17025.
- Strong understanding of principle of analytical chemistry and organic chemistry such as titration technic, GC, GC/MS and sample preparation technic.
- Proficiency in using SAP (QM module) and LIMS is highly desirable.
- Experience with a wide range of analytical laboratory techniques and instrumentation.
Key Responsibilities & Duties
Quality Management System (QMS) Leadership:
- Act as a key figure in the implementation and maintenance of the laboratory’s quality management system in accordance with ISO/IEC 17025 standards.
- Ensure all laboratory practices, documentation, and procedures are compliant with the standard.
Specification & Data Management:
- Manage and maintain all finished good specifications within the SAP system.
- Lead the ongoing implementation, maintenance, and user training for the Laboratory Information Management System (LIMS).
- Ensure data integrity and accurate reporting across all quality systems.
Product Release & Documentation:
- Meticulously review and provide final approval (signature) on Certificates of Analysis (COA) for all batches of finished goods.
- Compile, summarize, and deliver comprehensive traceability documentation as required by internal departments (e.g., Production, Supply Chain, Sales) to support inquiries and ensure full product recall readiness.
Laboratory Resource Management:
- Monitor and manage all laboratory resources, including analytical equipment, chemical reagents, apparatus, and personnel, to ensure operational efficiency.
- Proactively identify and manage the replacement of aging or malfunctioning equipment to prevent any negative impact on analysis accuracy.
- Create and process purchase requisitions for all laboratory requirements in alignment with ISO 17025 purchasing protocols.
Team Leadership & Development:
- Provide direct supervision, mentorship, and training to subordinate QC analysts and technicians.
- Develop training materials and conduct regular training sessions on test methods, safety procedures, and quality standards.
Internal & External Collaboration:
- Collaborate with other departments, such as Production and Marketing, to provide technical support for new product development and customer requirements.
- Assist the QA/QC Manager in investigating customer complaints and implementing corrective and preventive actions (CAPA).
General Duties:
- Support the QA/QC Manager in preparing for and participating in internal and external audits (customer, regulatory, certification).
- Perform other related duties and take on special projects as assigned by the QA/QC Manager to support departmental and company objectives.
